Last year, Shane’s grandson Finn Cadman stood before Parliament and spoke about the realities of MND. At just nine years old, he showed more courage and determination than many adults. Finn didn’t just accept his grandfather’s (Glampa’s) diagnosis, he turned his heartbreak into action, raising thousands of dollars and becoming an advocate for those who no longer have a voice.
His words carried weight because they came from a place of love and raw honesty. He wasn’t just speaking for Shane, he was speaking for every family impacted by MND, for those who have fought and those who will face this battle in the future.
We couldn’t be prouder of Finn and the impact he’s making. His determination reminds us all that while MND may be relentless, so too is the fight for awareness, support, and ultimately, a cure.